[Hiring] Patient Safety Associate I @Parexel

Role Description

We are seeking a Patient Safety Associate I (Pharmacovigilance Associate, Drug Safety Associate) to join our team. This role supports critical patient safety and pharmacovigilance activities that help ensure the safe and compliant development of therapies for patients worldwide.

As a Patient Safety Associate I, you will contribute to a broad range of safety operations, including:

• Individual case safety report processing
• Safety submissions
• Literature review activities
• Affiliate support
• Regulatory support
• Regulatory intelligence activities

Working within established procedures and under appropriate supervision, you will play an important role in maintaining compliance with global regulatory requirements and supporting the delivery of high-quality patient safety services.

You will gain exposure to a wide range of pharmacovigilance processes while collaborating with experienced professionals across global teams. This role offers an excellent opportunity to build expertise in drug safety, regulatory compliance, and clinical research while contributing to activities that help protect patients and support the development of innovative therapies.

Qualifications

• Strengths in organization, attention to detail, and analytical thinking
• An interest in pharmacovigilance, patient safety, pharmaceutical development, or healthcare environments
• The ability to collaborate effectively with team members and communicate clearly
• A patient-focused mindset and commitment to quality and compliance
• Experience working with pharmacovigilance systems, databases, Microsoft Office applications, and established workflows
• A strong desire to learn, develop new skills, and contribute to clinical research and patient safety initiatives

Requirements

• Bachelor’s degree in Life Sciences, Health Sciences, Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology) or equivalent education/experience
• Foundational knowledge of drug safety regulations and pharmacovigilance processes; ideal candidate has 3+ years experience in Drug Safety
• 2+ years experience in post marketing
• Experience in multiple therapeutic areas (cardiology, neurology, oncology, rare disease)
• Strong attention to detail, organizational skills, and problem-solving ability
• Effective communication and willingness to work in a collaborative team environment
• Proficiency with MS Office and ability to learn safety systems/databases; preference for those with Veeva Safety experience

Benefits

• Health, Vision & Dental Insurance
• Tuition Reimbursement
• Vacation/Holiday/Sick Time
• Flexible Spending & Health Savings Accounts
• Work/Life Balance
• 401(k) with Company match
• Pet Insurance

For a complete list of benefits, please visit www.parexel.com/us-benefits .

We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.

Company Description

Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.